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UnknownAge, race and viral genotype are associated with the prevalence of hepatitis B e antigen in children and adults with chronic hepatitis B.
Not available
S-EPMC6592737 | biostudies-literature
ProteomicsTgfbr2 in dental pulp cells guides neurite outgrowth in developing teeth
Transforming growth factor (TGF) plays an important role in tooth morphogenesis and mineralization. During postnatal development, the dental pulp (DP) mesenchyme secretes neurotrophic factors that guide trigeminal nerve fibers into and throughout the DP. This process is tightly linked with dentin f...
ORGANISM(S): Mus musculus (Mouse) 
2022-02-04 | PXD031046 | Pride
Dental pulp Neurotrophins Neurite outgrowth Tgfbeta signaling Trigeminal Tooth development Sensory innervation Semaphorins Tgfbeta 
UnknownProspective Study of Psychosocial Outcomes of Having Contralateral Prophylactic Mastectomy Among Women With Nonhereditary Breast Cancer.
Not available
S-EPMC6118404 | biostudies-literature
UnknownMedicare Part D Plans Rarely Cover Brand-Name Drugs When Generics Are Available.
Not available
S-EPMC9297534 | biostudies-literature
UnknownInfantile Myelofibrosis and Myeloproliferation with CDC42 Dysfunction.
Not available
S-EPMC7253386 | biostudies-literature
UnknownTrastuzumab deruxtecan versus trastuzumab emtansine in HER2-positive metastatic breast cancer patients with brain metastases from the randomized DESTINY-Breast03 trial.
Not available
S-EPMC11145752 | biostudies-literature
UnknownSociety for Immunotherapy of Cancer (SITC) clinical practice guideline on immunotherapy for the treatment of lung cancer and mesothelioma.
Not available
S-EPMC9157337 | biostudies-literature
GenomicsNHLBI GO-ESP: Lung Cohorts Exome Sequencing Project (Cystic Fibrosis): Genetic modifiers of Pseudomonas aeruginosa (Pa) lung infection acquisition in cystic fibrosis

The NHLBI "Grand Opportunity" Exome Sequencing Project (GO-ESP), a signature project of the NHLBI Recovery Act investment, was designed to identify genetic variants in coding regions (exons) of the human genome (the "exome") that are associated with heart, lung and blood diseases. These a...

phs000254.v1.p1 | EGA
GenomicsSporadic autism exomes reveal a highly interconnected protein network of de novo mutations

It is well established that autism spectrum disorders (ASD) have a strong genetic component; however, for at least 70% of cases, the underlying genetic cause is unknown. Under the hypothesis that de novo mutations underlie a substantial fraction of the risk for developing ASD in families with no ...

phs000482.v1.p1 | EGA
GenomicsGenetic Analysis of Limb Malformation Disorders: Freeman Sheldon Syndrome Exome Sequencing Study (LMD-FSS)

The overall goal of this project is to investigate the etiology and pathogenesis of malformations (i.e., birth defects) of the limb, concentrating on abnormalities of limb patterning such as limb deficiency/duplications and multiple congenital contractures.

The exome sequences of four ...

phs000204.v1.p1 | EGA
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